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- ...Job Summary We are seeking a QA Specialist with GMP experience to provide basic quality support for a pharmaceutical manufacturing environment. This role will support day-to-day quality assurance activities , with a strong focus on deviation management and GMP documentation...SuggestedContract work
- ...candidate will review documentation, conduct inspections, and maintain GMP compliance, contributing significantly to quality assurance... ...presents a great opportunity for individuals with a background in life sciences who aim to progress in a QA career. #J-18808-Ljbffr...Suggested
$65.25k - $169.4k
...products through effective quality oversight. The candidate will be responsible for performing final batch disposition and ensuring GMP compliance, as well as reviewing GMP documents. The ideal candidate holds a Bachelor’s degree in STEM, has experience in the pharmaceutical...SuggestedFull time- ...About the job GMP Quality Assurance Associate GMP Quality Assurance Associate needs 5+ years of GMP Quality Control Laboratory... ...and/or experience in API or finished product manufacturing, QA or Engineering. GMP Quality Assurance Associate requires:...Suggested
- ...assurance activities, inspecting products, and ensuring compliance with GMP standards. The ideal candidate should possess strong knowledge of... ..., effective communication skills, and a minimum of 3 years in a QA role. The position requires attention to detail and the ability...Suggested
$118k - $145k
Sonara Inc. in Maryland seeks a Lead Specialist in Client QA to oversee quality assurance for pharmaceutical projects. This role requires... ...collaboration with manufacturing teams to ensure compliance with GMP standards and successful project delivery. The ideal candidate...Suggested- Bristol Myers Squibb in Harvard, MA is seeking a Senior Specialist for Field Quality QA Operations. This role involves maintaining quality oversight, ensuring GMP compliance, and supporting real‑time quality assurance during manufacturing operations. The ideal candidate...SuggestedFull timeAfternoon shift
- KBI Biopharma Inc. in Durham, NC is seeking a Senior QA Specialist to oversee the review and approval of deviations and CAPAs supporting GMP manufacturing operations. The ideal candidate will have significant experience in the biopharmaceutical QA environment and will mentor...Suggested
- Eli Lilly and Company is seeking a Principal Associate QA-FUME in St. Louis, Missouri. This position is responsible for ensuring GMP compliance in facility oversight, utilities, maintenance, and equipment, essential for regulatory approvals. The ideal candidate will have...Suggested
$118k - $145k
Catalent is seeking a Lead Specialist, QA based in Harmans, Maryland. The role involves providing QA oversight on GMP manufacturing projects and ensuring compliance with quality standards. Candidates should have a relevant degree and experience in Quality Assurance/Quality...Suggested- ...assisting in the development of SOPs. The ideal candidate will have a Bachelor's degree in Chemistry or related field, ten years of GMP experience, and proven ability in aseptic manufacturing. This is a full-time on-site position with second shift hours. #J-18808-Ljbffr...SuggestedFull timeAfternoon shift
- BioSpace is seeking a Senior Associate Plant QA for the night shift in New Albany, Ohio. The role involves providing QA guidance and support to production, ensuring compliance with SOPs and GMP operations. Responsibilities include reviewing production records, mentoring...SuggestedFlexible hoursNight shift
$169.4k
...Quality Assurance professional. This position involves ensuring GMP compliance and performing batch disposition for pharmaceutical products... ...must have a Bachelor's degree in a STEM field and experience in QA roles, demonstrating strong technical decision-making skills and...Suggested$210k - $250k
...seeking a Director of Quality Assurance. This role is responsible for leading quality assurance functions, ensuring compliance with GMP standards, and overseeing regulatory adherence. Ideal candidates have 15+ years in quality management with a strong focus on the pharmaceutical...Suggested- Initial Therapeutics, Inc. is seeking a Principal Associate QA‑FUME in Houston. This pivotal role emphasizes quality oversight of facilities, utilities, and equipment for ensuring GMP compliance. The ideal candidate will possess at least 5 years of experience within the...Suggested
$74.96k - $103.07k
AGC Biologics in Bothell, Washington is seeking a QA Associate III to support GMP manufacturing by reviewing and approving key documentation. This role is critical for ensuring compliance and resolving issues on the manufacturing floor. The ideal candidate will have over...- ...quality system processes. Ideal candidates should have a Bachelor’s degree, over 7 years in quality assurance within biotech, and strong GMP knowledge. The position requires excellent technical writing skills and the ability to collaborate across functions. #J-18808-Ljbffr...
- ...seeking a Quality Specialist to ensure compliance with SOPs and QA standards. This role involves close collaboration with operations... ...2 years in pharmaceutical quality assurance. Strong knowledge of GMP and excellent problem-solving skills are essential. The position...
- Lonza Inc. in Portsmouth is seeking a QA Operations Specialist III to ensure compliance and provide real-time quality oversight in GMP manufacturing. Candidates should have 5-8 years of relevant experience in a cGMP-regulated environment and possess a bachelor's degree...Shift work
- ...in-house position involves microbiology testing and ensuring compliance with product specifications and GMP standards. The ideal candidate should have 5-10 years of QA experience, including management experience, and a strong understanding of microbiological testing...Full time
- ...Pharmaceutical GMP QA Specialist Synergy is seeking a detail-oriented and experienced Pharmaceutical GMP QA Specialist to ensure compliance with Good Manufacturing Practices (GMP) in pharmaceutical development and testing processes. The QA Specialist will be responsible...
- ...A pharmaceutical organization is seeking a QA Specialist with GMP experience for a one-year contract role located in Smyrna, GA. The candidate will provide fundamental quality assurance support, focusing on deviation management and GMP documentation in a regulated pharmaceutical...Contract work
- ...Qualifications include a Bachelor’s degree in Life Sciences or Engineering with at least 8 years of relevant experience, and prior work in a GMP environment. Candidates should have experience with validation software and a collaborative mindset. #J-18808-Ljbffr FUJIFILM...
- VARITE is looking for a qualified QA Specialist - II in Oceanside, CA. Job Title: Quality Assurance Specialist II Location: Oceanside... ...on-the-floor QA oversight and support to ensure compliance with GMP throughout the areas Perform walk-throughs and process observations...Contract workNight shift
$48k - $52k
...manufacturing processes. The role includes reviewing compliance with corporate SOPs and FDA guidelines, performing inspections, and monitoring GMP compliance. Qualified candidates should hold a Bachelor’s degree and possess 2 years of relevant experience in Quality Assurance or...$65.99k - $90.74k
...seeking a Quality Assurance Associate Specialist in East Windsor Township, NJ. This role focuses on ensuring FDA compliance, reviewing GMP documentation, and releasing Finished Goods. The ideal candidate has a bachelor's degree in Engineering or Science and at least two...$36 - $45 per hour
...assignment supporting quality and compliance activities within a GMP-regulated manufacturing environment. This hybrid position will provide... ...Environmental monitoring programs Cleanroom operations Provide QA oversight of aseptic processing activities to ensure compliance...Contract workTemporary workLocal area2 days per week3 days per week- ...Quality Assurance professional to manage quality standards in a GMP-regulated environment. This role involves overseeing the Quality... ...candidate should have a Bachelor's/Master's degree with 3-5 years of QA experience and a thorough understanding of cGMP regulations and...
- ...ideal candidate will have a Bachelor's degree in a scientific field and 3-5 years of relevant QA experience in a regulated environment. Responsibilities include conducting GMP investigations, managing quality metrics, providing hands-on training and support for FDA inspections...
- ...biotech sector and a Bachelor’s degree or higher. Responsibilities include reviewing batch records, assisting in audits, and ensuring adherence to GMP standards. This role promotes collaboration and strong communication skills in a dynamic team environment. #J-18808-Ljbffr...
